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Familial deletion within NLGN4 associated with autism and Tourette syndrome

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Familial deletion within NLGN4 associated with autism and Tourette syndrome (English)

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Amy Lawson-Yuen

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Juan-Sebastian Saldivar

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2

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Steve Sommer

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3

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Jonathan Picker

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4

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language of work or name

English

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publication date

May 2008

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published in

European Journal of Human Genetics

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volume

16

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issue

5

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page(s)

614-8

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cites work

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

21 January 2018

Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

21 January 2018

Neuroligin 1: a splice site-specific ligand for beta-neurexins

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The neuroligin and neurexin families: from structure to function at the synapse

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A splice code for trans-synaptic cell adhesion mediated by binding of neuroligin 1 to alpha- and beta-neurexins

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Neuroligins mediate excitatory and inhibitory synapse formation: involvement of PSD-95 and neurexin-1beta in neuroligin-induced synaptic specificity.

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

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7 January 2021

based on heuristic

inferred from DOI database lookup

Neuroligins determine synapse maturation and function

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

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7 January 2021

based on heuristic

inferred from DOI database lookup

Cartography of neurexins: more than 1000 isoforms generated by alternative splicing and expressed in distinct subsets of neurons.

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Structures, alternative splicing, and neurexin binding of multiple neuroligins

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a novel neuroligin in humans which binds to PSD-95 and has a widespread expression

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

High frequency of neurexin 1beta signal peptide structural variants in patients with autism

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of four neuroligin genes as candidates for autism.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Screening for Neuroligin 4 (NLGN4) truncating and transmembrane domain mutations in schizophrenia

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202006

retrieved

7 January 2021

based on heuristic

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(Q28266485)

Familial deletion within NLGN4 associated with autism and Tourette syndrome

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